SUNSCREEN

Manufacturer
Private Label Select Ltd CO
Effective date
2017-05-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:49:49

Label at a glance#

ProductSUNSCREEN
Active ingredientZINC OXIDE
Label structure2 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principalpanel labelcvsPrincipalpanel labelcvs

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

cvsblisterbccvsblisterbc

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62932-152-192020-01-31C16284748780-19d75b9d0-2908-f424-e053-dadaa90a57ce4f19f41f-3cef-0119-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62932-152-19SUNSCREEN1 in 1 BLISTER PACKSTICK11
62932-152-19SUNSCREEN19 g in 1 CONTAINERSTICK191

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62932-152SUNSCREEN (ZINC OXIDE SUNSCREEN) STICK [PRIVATE LABEL SELECT LTD CO]1Legacy NDC, 2 package rows20170510_4f19f41f-3cef-0119-e054-00144ff8d46c.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62932-15262932-152-19

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4f19f41f-3cf0-0119-e054-00144ff8d46c4f19f41f-3cef-0119-e054-00144ff8d46c2017-05-09Exact identifier
spl id: 4f19f41f-3cf0-0119-e054-00144ff8d46c
spl set id: 4f19f41f-3cef-0119-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.